Screening of renal anomalies in first-degree relatives of children diagnosed with non-syndromic congenital anomalies of kidney and urinary tract
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Nephrology,Physiology
Link
https://link.springer.com/content/pdf/10.1007/s10157-020-01977-7.pdf
Reference29 articles.
1. Bulum B, Ozçakar ZB, Ustüner E, Düşünceli E, Kavaz A, Duman D, et al. High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT. Pediatr Nephrol Berl Ger. 2013;28:2143–7.
2. Soliman NA, Ali RI, Ghobrial EE, Habib EI, Ziada AM. Pattern of clinical presentation of congenital anomalies of the kidney and urinary tract among infants and children. Nephrol Carlton Vic. 2015;20:413–8.
3. Suman Gök E, Ayvacı A, Ağbaş A, Adaletli İ, Canpolat N, Sever L, et al. The Frequency of Familial Congenital Anomalies of the Kidney and Urinary Tract: Should We Screen Asymptomatic First-Degree Relatives Using Urinary Tract Ultrasonography? Nephron. 2020;1–6.
4. Yosypiv IV. Congenital anomalies of the kidney and urinary tract: a genetic disorder? Int J Nephrol. 2012;2012:909083.
5. Beke A, Eros FR, Pete B, Szabo I, Gorbe E, Rigo J. Efficacy of prenatal ultrasonography in diagnosing urogenital developmental anomalies in newborns. BMC Pregnancy Childbirth. 2014;14:82.
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Practical Approach to Congenital Anomalies of the Kidneys: Focus on Anomalies With Insufficient or Abnormal Nephron Development: Renal Dysplasia, Renal Hypoplasia, and Renal Tubular Dysgenesis;Pediatric and Developmental Pathology;2024-09-13
2. GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract;Human Genomics;2024-04-24
3. Brain and spine malformations and neurodevelopmental disorders in a cohort of children with CAKUT;Pediatric Nephrology;2024-02-20
4. The genetics and pathogenesis of CAKUT;Nature Reviews Nephrology;2023-07-31
5. Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-09
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3